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The work between your data and your decision.

We curate the data, run the analysis, and build the systems that do it again.

Colour by

2,200 simulated cells, embedded from a 240-gene expression matrix. Pick a population, or colour the field by a marker gene.

Every result arrives with the reasoning attached

Anyone can produce a plot. What makes it usable a year later is knowing which decisions produced it, which of those were close calls, and what would have to be true for the conclusion to fail.

A plan before a pipeline

The design, the covariates, the tests, and the thresholds are written down and agreed before anything runs. Analyses that decide their own hypotheses afterwards are not analyses.

Reproducible from raw

Versioned code and a pinned environment that regenerate every figure in the report from the original inputs, on your machine, without us.

Limits, stated

Each conclusion arrives with what it rests on, what would overturn it, and which questions the data was never going to answer.

What we take on

  • Curation and harmonisation of omics data and its metadata
  • Bulk, single-cell, spatial, and proteomic analysis end to end
  • Agentic and non-agentic scientific software, built to be handed over
  • In-silico research programmes that produce testable hypotheses

What we do not

  • Wet lab work of any kind, including validation experiments
  • Sequencing, sample handling, or primary data generation
  • Regulatory submissions and GxP-validated pipelines
  • Clinical trial operations or patient-facing systems

We work with the groups who do, and will say so early rather than late.

Tell us what you are trying to find out

Send the shape of the data and the decision that depends on it. You get an honest read on whether the question is answerable before anyone talks about scope.